Canonical Allele Identifier: PA2573170434
Gene: CFTR HGNC NCBI

Linked Data

ClinVar Variation Id: 1467947

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000483.3:p.Gly126Ala
CA368974527
NM_000492.4:c.377G>C